-
1
-
-
55549136382
-
Diagnosis and classification of myelodysplastic syndrome: International Working Group on Morphology of myelodysplastic syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts
-
Mufti G. J., et al. Diagnosis and classification of myelodysplastic syndrome: International Working Group on Morphology of myelodysplastic syndrome (IWGM-MDS) consensus proposals for the definition and enumeration of myeloblasts and ring sideroblasts. Haematologica 93, 1712-1717 (2008
-
(2008)
Haematologica
, vol.93
, pp. 1712-1717
-
-
Mufti, G.J.1
-
3
-
-
80053900941
-
Frequent pathway mutations of splicing machinery in myelodysplasia
-
Yoshida K., et al. Frequent pathway mutations of splicing machinery in myelodysplasia. Nature 478, 64-69 (2011
-
(2011)
Nature
, vol.478
, pp. 64-69
-
-
Yoshida, K.1
-
4
-
-
84879565619
-
Spliceosome mutations exhibit specific associations with epigenetic modifiers and proto-oncogenes mutated in myelodysplastic syndrome
-
Mian S. A., et al. Spliceosome mutations exhibit specific associations with epigenetic modifiers and proto-oncogenes mutated in myelodysplastic syndrome. Haematologica 98, 1058-1066 (2013
-
(2013)
Haematologica
, vol.98
, pp. 1058-1066
-
-
Mian, S.A.1
-
5
-
-
80054010617
-
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts
-
Papaemmanuil E., et al. Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts. N. Engl. J. Med. 365, 1384-1395 (2011
-
(2011)
N. Engl. J. Med
, vol.365
, pp. 1384-1395
-
-
Papaemmanuil, E.1
-
6
-
-
84860767817
-
SF3B1 mutations in myelodysplastic syndromes: Clinical associations and prognostic implications
-
Damm F., et al. SF3B1 mutations in myelodysplastic syndromes: clinical associations and prognostic implications. Leukemia 26, 1137-1140 (2012
-
(2012)
Leukemia
, vol.26
, pp. 1137-1140
-
-
Damm, F.1
-
7
-
-
84868091622
-
SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes
-
Visconte V., et al. SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes. Blood 120, 3173-3186 (2012
-
(2012)
Blood
, vol.120
, pp. 3173-3186
-
-
Visconte, V.1
-
8
-
-
84893772765
-
Landscape of genetic lesions in 944 patients with myelodysplastic syndromes
-
Haferlach T., et al. Landscape of genetic lesions in 944 patients with myelodysplastic syndromes. Leukemia 28, 241-247 (2014
-
(2014)
Leukemia
, vol.28
, pp. 241-247
-
-
Haferlach, T.1
-
9
-
-
14644431836
-
Mammalian polycomb-mediated repression of Hox genes requires the essential spliceosomal protein Sf3b1
-
Isono K., Mizutani-Koseki Y., Komori T., Schmidt-Zachmann M. S., & Koseki H. Mammalian polycomb-mediated repression of Hox genes requires the essential spliceosomal protein Sf3b1. Genes Dev. 19, 536-541 (2005
-
(2005)
Genes Dev
, vol.19
, pp. 536-541
-
-
Isono, K.1
Mizutani-Koseki, Y.2
Komori, T.3
Schmidt-Zachmann, M.S.4
Koseki, H.5
-
10
-
-
84856013431
-
Clonal evolution in cancer
-
Greaves M., & Maley C. C. Clonal evolution in cancer. Nature 481, 306-313 (2012
-
(2012)
Nature
, vol.481
, pp. 306-313
-
-
Greaves, M.1
Maley, C.C.2
-
11
-
-
69449096005
-
Heterogeneity in cancer: Cancer stem cells versus clonal evolution
-
Shackleton M., Quintana E., Fearon E. R., & Morrison S. J. Heterogeneity in cancer: cancer stem cells versus clonal evolution. Cell 138, 822-829 (2009
-
(2009)
Cell
, vol.138
, pp. 822-829
-
-
Shackleton, M.1
Quintana, E.2
Fearon, E.R.3
Morrison, S.J.4
-
12
-
-
84867121875
-
Intratumor heterogeneity: Evolution through space and time
-
Swanton C. Intratumor heterogeneity: evolution through space and time. Cancer Res. 72, 4875-4882 (2012
-
(2012)
Cancer Res
, vol.72
, pp. 4875-4882
-
-
Swanton, C.1
-
13
-
-
78751644099
-
Genetic variegation of clonal architecture and propagating cells in leukaemia
-
Anderson K., et al. Genetic variegation of clonal architecture and propagating cells in leukaemia. Nature 469, 356-361 (2011
-
(2011)
Nature
, vol.469
, pp. 356-361
-
-
Anderson, K.1
-
14
-
-
84896081834
-
Functional heterogeneity of genetically defined subclones in acute myeloid leukemia
-
Klco J. M., et al. Functional heterogeneity of genetically defined subclones in acute myeloid leukemia. Cancer Cell. 25, 379-392 (2014
-
(2014)
Cancer Cell
, vol.25
, pp. 379-392
-
-
Klco, J.M.1
-
15
-
-
84902480315
-
Myelodysplastic syndromes are propagated by rare and distinct human cancer stem cells in vivo
-
Woll P. S., et al. Myelodysplastic syndromes are propagated by rare and distinct human cancer stem cells in vivo. Cancer Cell. 25, 794-808 (2014
-
(2014)
Cancer Cell
, vol.25
, pp. 794-808
-
-
Woll, P.S.1
-
16
-
-
84859597590
-
Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
-
Makishima H., et al. Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis. Blood 119, 3203-3210 (2012
-
(2012)
Blood
, vol.119
, pp. 3203-3210
-
-
Makishima, H.1
-
17
-
-
84896689530
-
Identification of a novel erythroid-specific enhancer for the ALAS2 gene and its loss-of-function mutation which is associated with congenital sideroblastic anemia
-
Kaneko K., et al. Identification of a novel erythroid-specific enhancer for the ALAS2 gene and its loss-of-function mutation which is associated with congenital sideroblastic anemia. Haematologica 99, 252-261 (2014
-
(2014)
Haematologica
, vol.99
, pp. 252-261
-
-
Kaneko, K.1
-
18
-
-
0033105568
-
Four new mutations in the erythroid-specific 5- aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: Increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis
-
Cotter P. D., et al. Four new mutations in the erythroid-specific 5- aminolevulinate synthase (ALAS2) gene causing X-linked sideroblastic anemia: increased pyridoxine responsiveness after removal of iron overload by phlebotomy and coinheritance of hereditary hemochromatosis. Blood 93, 1757-1769 (1999
-
(1999)
Blood
, vol.93
, pp. 1757-1769
-
-
Cotter, P.D.1
-
19
-
-
70349335786
-
Hereditary sideroblastic anemias: Pathophysiology, diagnosis, and treatment
-
Camaschella C. Hereditary sideroblastic anemias: pathophysiology, diagnosis, and treatment. Semin Hematol. 46, 371-377 (2009
-
(2009)
Semin Hematol
, vol.46
, pp. 371-377
-
-
Camaschella, C.1
-
20
-
-
84888219405
-
Clinical and biological implications of driver mutations in myelodysplastic syndromes
-
Papaemmanuil E., et al. Clinical and biological implications of driver mutations in myelodysplastic syndromes. Blood 122, 3616-3627 (2013
-
(2013)
Blood
, vol.122
, pp. 3616-3627
-
-
Papaemmanuil, E.1
-
21
-
-
84866749552
-
Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes
-
Bejar R., et al. Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes. J. Clin. Oncol. 30, 3376-3382 (2012
-
(2012)
J. Clin. Oncol
, vol.30
, pp. 3376-3382
-
-
Bejar, R.1
-
22
-
-
84874235360
-
Hematopoietic stem cell and progenitor cell mechanisms in myelodysplastic syndromes
-
Pang W. W., et al. Hematopoietic stem cell and progenitor cell mechanisms in myelodysplastic syndromes. Proc. Natl Acad. Sci. USA 110, 3011-3016 (2013
-
(2013)
Proc. Natl Acad. Sci. USA
, vol.110
, pp. 3011-3016
-
-
Pang, W.W.1
-
23
-
-
79960106880
-
Isolation of single human hematopoietic stem cells capable of long-term multilineage engraftment
-
Notta F., et al. Isolation of single human hematopoietic stem cells capable of long-term multilineage engraftment. Science 333, 218-221 (2011
-
(2011)
Science
, vol.333
, pp. 218-221
-
-
Notta, F.1
-
24
-
-
0030789242
-
Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell
-
Bonnet D., & Dick J. E. Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell. Nat. Med. 3, 730-737 (1997
-
(1997)
Nat. Med
, vol.3
, pp. 730-737
-
-
Bonnet, D.1
Dick, J.E.2
-
25
-
-
84902200836
-
Myelodysplastic cells in patients reprogram mesenchymal stromal cells to establish a transplantable stem cell niche disease unit
-
Medyouf H., et al. Myelodysplastic cells in patients reprogram mesenchymal stromal cells to establish a transplantable stem cell niche disease unit. Cell Stem Cell 14, 824-837 (2014
-
(2014)
Cell Stem Cell
, vol.14
, pp. 824-837
-
-
Medyouf, H.1
-
26
-
-
20144388146
-
Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer
-
Fraga M. F., et al. Loss of acetylation at Lys16 and trimethylation at Lys20 of histone H4 is a common hallmark of human cancer. Nat. Genet. 37, 391-400 (2005
-
(2005)
Nat. Genet
, vol.37
, pp. 391-400
-
-
Fraga, M.F.1
-
27
-
-
32544452237
-
Loss of DNA methylation and histone H4 lysine 20 trimethylation in human breast cancer cells is associated with aberrant expression of DNA methyltransferase 1, Suv4-20h2 histone methyltransferase and methyl-binding proteins
-
Tryndyak V. P., Kovalchuk O., & Pogribny I. P. Loss of DNA methylation and histone H4 lysine 20 trimethylation in human breast cancer cells is associated with aberrant expression of DNA methyltransferase 1, Suv4-20h2 histone methyltransferase and methyl-binding proteins. Cancer Biol. Ther. 5, 65-70 (2006
-
(2006)
Cancer Biol. Ther
, vol.5
, pp. 65-70
-
-
Tryndyak, V.P.1
Kovalchuk, O.2
Pogribny, I.P.3
-
28
-
-
84862776906
-
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
-
Ding L., et al. Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. Nature 481, 506-510 (2012
-
(2012)
Nature
, vol.481
, pp. 506-510
-
-
Ding, L.1
-
29
-
-
70149093912
-
Recurring mutations found by sequencing an acute myeloid leukemia genome
-
Mardis E. R., et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N. Engl. J. Med. 361, 1058-1066 (2009
-
(2009)
N. Engl. J. Med
, vol.361
, pp. 1058-1066
-
-
Mardis, E.R.1
-
30
-
-
84864255882
-
The origin and evolution of mutations in acute myeloid leukemia
-
Welch J. S., et al. The origin and evolution of mutations in acute myeloid leukemia. Cell 150, 264-278 (2012
-
(2012)
Cell
, vol.150
, pp. 264-278
-
-
Welch, J.S.1
-
31
-
-
79960255863
-
Recurrent DNMT3A mutations in patients with myelodysplastic syndromes
-
Walter M. J., et al. Recurrent DNMT3A mutations in patients with myelodysplastic syndromes. Leukemia 25, 1153-1158 (2011
-
(2011)
Leukemia
, vol.25
, pp. 1153-1158
-
-
Walter, M.J.1
-
32
-
-
34548827379
-
Suv4-20h deficiency results in telomere elongation and derepression of telomere recombination
-
Benetti R., et al. Suv4-20h deficiency results in telomere elongation and derepression of telomere recombination. J. Cell Biol. 178, 925-936 (2007
-
(2007)
J. Cell Biol
, vol.178
, pp. 925-936
-
-
Benetti, R.1
-
33
-
-
77950451485
-
Leukemia-initiating cells from some acute myeloid leukemia patients with mutated nucleophosmin reside in the CD34(-) fraction
-
Taussig D. C., et al. Leukemia-initiating cells from some acute myeloid leukemia patients with mutated nucleophosmin reside in the CD34(-) fraction. Blood 115, 1976-1984 (2010
-
(2010)
Blood
, vol.115
, pp. 1976-1984
-
-
Taussig, D.C.1
-
34
-
-
50949090415
-
Anti-CD38 antibody-mediated clearance of human repopulating cells masks the heterogeneity of leukemia-initiating cells
-
Taussig D. C., et al. Anti-CD38 antibody-mediated clearance of human repopulating cells masks the heterogeneity of leukemia-initiating cells. Blood 112, 568-575 (2008
-
(2008)
Blood
, vol.112
, pp. 568-575
-
-
Taussig, D.C.1
-
35
-
-
78651416188
-
Coexistence of LMPP-like and GMP-like leukemia stem cells in acute myeloid leukemia
-
Goardon N., et al. Coexistence of LMPP-like and GMP-like leukemia stem cells in acute myeloid leukemia. Cancer Cell 19, 138-152 (2011
-
(2011)
Cancer Cell
, vol.19
, pp. 138-152
-
-
Goardon, N.1
-
36
-
-
84872706645
-
Functional characterization of T cell populations in a mouse model of chronic obstructive pulmonary disease
-
Eppert B. L., Wortham B. W., Flury J. L., & Borchers M. T. Functional characterization of T cell populations in a mouse model of chronic obstructive pulmonary disease. J. Immunol. 190, 1331-1340 (2013
-
(2013)
J. Immunol
, vol.190
, pp. 1331-1340
-
-
Eppert, B.L.1
Wortham, B.W.2
Flury, J.L.3
Borchers, M.T.4
-
37
-
-
67649884743
-
Fast and accurate short read alignment with Burrows- Wheeler transform
-
Li H., & Durbin R. Fast and accurate short read alignment with Burrows- Wheeler transform. Bioinformatics 25, 1754-1760 (2009
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
38
-
-
77956295988
-
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna A., et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res. 20, 1297-1303 (2010
-
(2010)
Genome Res
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
-
39
-
-
84863229597
-
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
-
Koboldt D. C., et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Res. 22, 568-576 (2012
-
(2012)
Genome Res
, vol.22
, pp. 568-576
-
-
Koboldt, D.C.1
-
40
-
-
69949122158
-
VarScan: Variant detection in massively parallel sequencing of individual and pooled samples
-
Koboldt D. C., et al. VarScan: variant detection in massively parallel sequencing of individual and pooled samples. Bioinformatics 25, 2283-2285 (2009
-
(2009)
Bioinformatics
, vol.25
, pp. 2283-2285
-
-
Koboldt, D.C.1
-
41
-
-
68549104404
-
The Sequence alignment/map format and SAMtools
-
Li H., et al. The Sequence alignment/map format and SAMtools. Bioinformatics 25, 2078-2079 (2009
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
-
42
-
-
70350694443
-
Pindel: A pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
-
Ye K., Schulz M. H., Long Q., Apweiler R., & Ning Z. Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads. Bioinformatics 25, 2865-2871 (2009
-
(2009)
Bioinformatics
, vol.25
, pp. 2865-2871
-
-
Ye, K.1
Schulz, M.H.2
Long, Q.3
Apweiler, R.4
Ning, Z.5
-
43
-
-
77956534324
-
Annovar: Functional annotation of genetic variants from high-throughput sequencing data
-
Wang K., Li M., & Hakonarson H. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res. 38, e164 (2010
-
(2010)
Nucleic Acids Res
, vol.38
, pp. e164
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
44
-
-
34447321852
-
Enhancements and modifications of primer design program Primer3
-
Koressaar T., & Remm M. Enhancements and modifications of primer design program Primer3. Bioinformatics 23, 1289-1291 (2007
-
(2007)
Bioinformatics
, vol.23
, pp. 1289-1291
-
-
Koressaar, T.1
Remm, M.2
|